71721-74-9Relevant articles and documents
Lipophilic NHC assisted one-pot synthesis of syncarpamide analogues in aqueous medium
Suresh, Pavithira,Selva Ganesan, Subramaniapillai
supporting information, p. 6257 - 6261 (2019/04/25)
Lipophilic NHC catalysis in aqueous medium was reported for the synthesis of biologically relevant (a)symmetrically substituted and unsymmetrically substituted syncarpamide analogues. All the reported reactions were performed in the absence of any expensive metal salts or additives. A diverse array of syncarpamide analogues was obtained in good yields. Lipophilic NHC catalysis was also extended to chemoselective transesterification reactions.
Olefins from biomass feedstocks: Catalytic ester decarbonylation and tandem Heck-type coupling
John, Alex,Hogan, Levi T.,Hillmyer, Marc A.,Tolman, William B.
supporting information, p. 2731 - 2733 (2015/03/05)
With the goal of avoiding the need for anhydride additives, the catalytic decarbonylation of p-nitrophenylesters of aliphatic carboxylic acids to their corresponding olefins, including commodity monomers like styrene and acrylates, has been developed. The reaction is catalyzed by palladium complexes in the absence of added ligands and is promoted by alkali/alkaline-earth metal halides. Combination of catalytic decarbonylation and Heck-type coupling with aryl esters in a single pot process demonstrates the viability of employing a carboxylic acid as a "masked olefin" in synthetic processes. This journal is
Synthesis and antimycobacterial evaluation of new trans-cinnamic acid hydrazide derivatives
Carvalho, Samir A.,da Silva, Edson F.,de Souza, Marcus V.N.,Lourenco, Maria C.S.,Vicente, Felipe R.
, p. 538 - 541 (2008/09/20)
In this work, we report the synthesis and the antimycobacterial evaluation of new trans-cinnamic acid derivatives of isonicotinic acid series (5) and benzoic acid series (6), designed by exploring the molecular hybridization approach between isoniazid (1)
